DOI:
10.1055/s-00025479
Experimental and Clinical Endocrinology & Diabetes Reports
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References
Louw JJ, Corveleyn A, Jia Y. et al.
Homozygous loss-of-function mutation in ALMS1 caues the lethal disorder mitogenic cardiomyopathy in two siblings.
Eur J Med Gene-t 2014;
57: 532-535
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